Division of Perioperative Services, Intensive Care and Pain Medicine, Turku University Hospital.
Department of Anesthesiology and Intensive Care.
J Hypertens. 2023 Mar 1;41(3):380-387. doi: 10.1097/HJH.0000000000003336. Epub 2022 Dec 16.
Preexisting hypertension increases risk for preeclampsia. We examined whether a generic blood pressure polygenic risk score (BP-PRS), compared with a preeclampsia-specific polygenic risk score (PE-PRS), could better predict hypertensive disorders of pregnancy.
Our study sample included 141 298 genotyped FinnGen study participants with at least one childbirth and followed from 1969 to 2021. We calculated PRSs for SBP and preeclampsia using summary statistics for greater than 1.1 million single nucleotide polymorphisms.
We observed 8488 cases of gestational hypertension (GHT) and 6643 cases of preeclampsia. BP-PRS was associated with GHT [multivariable-adjusted hazard ratio for 1SD increase in PRS (hazard ratio 1.38; 95% CI 1.35-1.41)] and preeclampsia (1.26, 1.23-1.29), respectively. The PE-PRS was also associated with GHT (1.16; 1.14-1.19) and preeclampsia (1.21, 1.18-1.24), but with statistically more modest magnitudes of effect (P = 0.01). The model c-statistic for preeclampsia improved when PE-PRS was added to clinical risk factors (P = 4.6 × 10-15). Additional increment in the c-statistic was observed when BP-PRS was added to a model already including both clinical risk factors and PE-PRS (P = 1.1 × 10-14).
BP-PRS is strongly associated with hypertensive disorders of pregnancy. Our current observations suggest that the BP-PRS could capture the genetic architecture of preeclampsia better than the current PE-PRSs. These findings also emphasize the common pathways in the development of all BP disorders. The clinical utility of a BP-PRS for preeclampsia prediction warrants further investigation.
既往高血压会增加子痫前期的风险。我们研究了一般的血压多基因风险评分(BP-PRS)与子痫前期特异性多基因风险评分(PE-PRS)相比,是否能更好地预测妊娠高血压疾病。
我们的研究样本包括 141298 名在芬兰基因研究中至少生育过一次的基因分型参与者,从 1969 年至 2021 年进行随访。我们使用超过 110 万个单核苷酸多态性的汇总统计数据计算 SBP 和子痫前期的 PRS。
我们观察到 8488 例妊娠期高血压(GHT)和 6643 例子痫前期病例。BP-PRS 与 GHT 相关(PRS 每增加 1SD 的多变量校正风险比为 1.38;95%CI 为 1.35-1.41)和子痫前期(1.26,1.23-1.29)。PE-PRS 也与 GHT(1.16;1.14-1.19)和子痫前期(1.21,1.18-1.24)相关,但效应的统计学幅度较小(P=0.01)。当将 PE-PRS 添加到临床危险因素时,子痫前期的模型 c 统计量得到改善(P=4.6×10-15)。当将 BP-PRS 添加到已经包括临床危险因素和 PE-PRS 的模型中时,c 统计量的额外增加是可见的(P=1.1×10-14)。
BP-PRS 与妊娠高血压疾病密切相关。我们目前的观察结果表明,BP-PRS 可能比当前的 PE-PRS 更好地捕捉子痫前期的遗传结构。这些发现还强调了所有 BP 疾病发展中的共同途径。BP-PRS 预测子痫前期的临床应用价值需要进一步研究。